IP Library Granted Patent US 10,213,417
Granted Patent B2
US 10,213,417 · App. 15/662,024 · Granted Feb 26, 2019

Fatty acids as anti-inflammatory agents

Inventors: Bruce A. Freeman (Pittsburgh, PA); Francisco J. Schopfer (Pittsburgh, PA)
Assignee: University of Pittsburgh—Of the Commonwealth System of Higher Education
A61K31/426A61K31/12A61K31/231A61K31/232A61K31/4166A61K31/4192A61K31/421Y02A50/401
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Quick Facts
Patent No.
US 10,213,417
App. No.
15/662,024
Granted
Feb 26, 2019
Kind
B2
Abstract

Compounds of formula I and their metabolites are potent mediators of an inflammatory response: where a, b, c, d, e, f, V, W, X, Y, R a , R a′ , R b , R b′ , R c , and R c′ are defined herein. In particular, the compounds of the invention are candidate therapeutics for treating inflammatory conditions.

Claims (43)

1. A method of treating an inflammatory condition comprising administering to the subject in need thereof a formulation comprising a therapeutically effective amount of a compound having the formula:

wherein:

R 1 is a heterocyclyl;

is an optional double bond;

W is —OH, —C(O)H, —C(O), —C(O)R p , —COOH, —COOR p , —Cl, —Br, —I, —CF 3 , —CN, —SO 3 , —SO 2 R p , —SO 3 H, —NH 3 +, —NH 2 R p+ , —NR p R q R t , —NO 2 , ═O, ═NR p , ═CF 2 , or —CHF;

each V is, independently —CH or —C—, wherein:

V is —CH— when W is —OH, —H, —C(O)H, —C(O), —C(O)R p , —COOH, —COOR p , —Cl, —Br, —I, —F, —CF 3 , —CN, —SO 3 , —SO 2 R p , —SO 3 H, —NH 3+ , —NH 2 R p+ , —NR p R q R t or —NO 2 ; or

V is —C— when W is ═O, ═NR p , ═CF 2 or ═CHF;

R p and R q are each, independently, H, (C 1 -C 8 ) alkyl, aryl, or (C 1 -C 8 ) haloalkyl;

R t is (C 1 -C 8 ) alkyl, aryl, or (C 1 -C 8 ) haloalkyl;

R b and R b′ are each independently, —H, —OH, —C(O)H, —C(O), —C(O)R p , —COOH, —COOR p , —Cl, —Br, —I, —F, —CF 3 , —CHF 2 , —CH 2 F, —CN, —SO 3 , —SO 2 R p , SO 3 H, —NH 3 + , —NH 2 R p+ , —NR p R q R t or —NO 2 , wherein:

R b and R b′ are not simultaneously non-hydrogen groups;

a is an integer between 5 and 15 inclusive, c is an integer from 1 and 15 inclusive, and f is an integer between 5 and 15 inclusive; and

a pharmaceutically acceptable carrier.

2. The method according to claim 1 , wherein W is —H, ═O or ═NR p .

3. The method according to claim 1 , wherein V is —CH— and W is —H.

4. The method according to claim 1 , wherein V is —C— and W is ═O.

5. The method according to claim 1 , wherein c is 1, V is —C—, and W is ═O.

6. The method according to claim 1 , wherein R b and R b′ , are each, independently, —H, —OH, —CN, or —NO 2 .

7. The method according to claim 1 , wherein R b and R b′ are each —H.

8. The method according to claim 1 , wherein a is 3.

9. The method to claim 1 , wherein R 1 is a heteroaryl or a heterocycloalkyl.

10. The method according to claim 1 , wherein the pharmaceutically acceptable carrier comprises a solid, solution, powder, fluid emulsion, fluid suspension, semi-solid, or dry powder.

11. The method according to claim 1 , further comprising at least one pharmaceutically acceptable diluent, filler, disintegrant, binder, lubricant, surfactant, hydrophobic vehicle, water soluble vehicle, emulsifier, buffer, humectant, moisturizer, solubilizer, antioxidant, or preservative, or a combination thereof.

12. The method according to claim 1 , wherein the inflammatory condition being treated is selected from the group consisting of pulmonary fibrosis, pulmonary inflammation, asthma, acquired respiratory distress syndrome, tobacco induced lung disease and chronic obstructive pulmonary disease.

13. A method of treating pulmonary inflammation in a subject comprising administering to a subject in need thereof a compound having a formula of:

wherein:

R 1 is a heterocyclyl;

is an optional double bond;

W is —OH, —C(O)H, —C(O), —C(O)R p , —COOH, —COOR p , —Cl, —Br, —I, —CF 3 , —CN, —SO 3 , —SO 2 R p , —SO 3 H, —NH 3 + , —NH 2 R p+ , —NR p R q R t , —NO 2 , ═O, ═NR p , ═CF 2 , or —CHF;

each V is, independently —CH or —C—, wherein:

V is —CH— when W is —OH, —H, —C(O)H, —C(O), —C(O)R p , —COOH, —COOR p , —Cl, —Br, —I, —F, —CF 3 , —CN, —SO 3 , —SO 2 R p , —SO 3 H, —NH 3 + , —NH 2 R p+ , —NR p R q R t or —NO 2 ; or

V is —C— when W is ═O, ═NR p , ═CF 2 or ═CHF;

R p and R q are each, independently, H, (C 1 -C 8 ) alkyl, aryl, or (C 1 -C 8 ) haloalkyl;

R t is (C 1 -C 8 ) alkyl, aryl, or (C 1 -C 8 ) haloalkyl;

R b and R b′ are each independently, —H, —OH, —C(O)H, —C(O), —C(O)R p , —COOH, —COOR p , —Cl, —Br, —I, —F, —CF 3 , —CHF 2 , —CH 2 F, —CN, —SO 3 , —SO 2 R p , SO 3 H, —NH 3 + , —NH 2 R p+ , —NR p R q R t or —NO 2 , wherein:

R b and R b′ are not simultaneously non-hydrogen groups;

a is an integer between 5 and 15 inclusive, c is an integer from 1 and 15 inclusive, and f is an integer between 5 and 15 inclusive.

14. The method according to claim 13 , wherein W is ═O or ═NR p .

15. The method according to claim 14 , wherein R 1 is a heteroaryl or a heterocycloalkyl.

16. The method according to claim 14 , wherein V is —C— and W is ═O.

17. The method according to claim 14 , wherein c is 1.

18. The method according to claim 13 , wherein the pulmonary inflammation is further selected from the group consisting of pulmonary fibrosis, asthma, acquired respiratory distress syndrome, tobacco induced lung disease and chronic obstructive pulmonary disease.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2017
From: FREEMAN, BRUCE A.; SCHOPFER, FRANCISCO J.
To: UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
Reel/Frame 043134/0640 →
Continuity (4)
Continuation 14717954 · May 20, 2015
Continuation 13387489
Provisional Application 61213946 · Jul 31, 2009
Related Publication 20180008580A1 · Jan 11, 2018
Cited By (2)
US 12,390,435 US 12,728,111